Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115568G>C , CM000681.2:g.10115568G>C | GRCh38 |
| NC_000019.9:g.10226244G>C , CM000681.1:g.10226244G>C | GRCh37 |
| NC_000019.8:g.10087244G>C | NCBI36 |
| NG_047007.1:g.9048G>C | |
| NG_051197.1:g.9357C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.858C>G MANE Select | ENSP00000253108.3:p.Ser286Arg | |
| ENST00000253108.8:c.858C>G | ENSP00000253108.3:p.Ser286Arg | |
| ENST00000589454.5:c.834C>G | ENSP00000466860.1:p.Ser278Arg | |
| ENST00000590158.1:n.877C>G | ||
| ENST00000593054.5:c.252C>G | ENSP00000467187.1:p.Ser84Arg | |
| NM_003755.3:c.858C>G | NP_003746.2:p.Ser286Arg | |
| NM_003755.4:c.858C>G | NP_003746.2:p.Ser286Arg | |
| NM_003755.5:c.858C>G MANE Select | NP_003746.2:p.Ser286Arg |